Sporadic inclusion body myositis

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Sporadic inclusion body myositis misdiagnosed as idiopathic granulomatous myositis

Neuromuscular Disorders, 2016
We present a case of a 65-year-old woman who was previously diagnosed with idiopathic granulomatous myositis and treated with immunosuppressive therapy for the next 10 years before a clinical diagnosis of inclusion body myositis was made. A review of the previously performed muscle biopsy showed most of the cardinal myopathologic features of sporadic ...
Monica, Lavian, Namita, Goyal, Tahseen, Mozaffar +2 more
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[Sporadic Inclusion Body Myositis].

Brain and nerve = Shinkei kenkyu no shinpo, 2023
Inclusion body myositis (IBM) is an idiopathic inflammatory muscle disease that predominantly affects elderly men over the age of 50 years, and the number of patients is rapidly increasing in Japan. Generally, muscle weakness and atrophy occur asymmetrically in the flexor muscles of the fingers and wrists and the quadriceps muscles.
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[Sporadic Inclusion Body Myositis and Autoantibodies].

Brain and nerve = Shinkei kenkyu no shinpo, 2019
Sporadic inclusion body myositis (sIBM) is a chronically progressing inflammatory myopathy most common in the aged population. Asymmetric muscle weakness and waste of the quadriceps and finger and wrist flexor muscles are characteristic features of sIBM.
Satoshi, Yamashita, Yukio, Ando
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Sporadic inclusion body myositis presenting with severe camptocormia

Journal of Clinical Neuroscience, 2013
Sporadic inclusion body myositis (sIBM) is a slowly progressive idiopathic inflammatory myopathy. The characteristic early quadriceps and finger flexor muscle weakness often leads to the diagnosis of sIBM, especially when all canonical pathological features of sIBM are not present on muscle biopsy.
Haihan, Ma +2 more
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Diagnosis and classification of sporadic inclusion body myositis (sIBM)

Autoimmunity Reviews, 2014
Sporadic inclusion body myositis (sIBM) is the most common acquired muscle disease in elderly individuals, particularly men. Its prevalence varies among ethnic groups but is estimated at 35 per one million people over 50. Genetic as well as environmental factors and autoimmune processes might both have a role in its pathogenesis.
M, Catalán, A, Selva-O'Callaghan, J M, Grau +2 more
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[Sporadic inclusion body myositis in Japan].

Nihon rinsho. Japanese journal of clinical medicine, 2012
Sporadic inclusion body myositis (sIBM), the most common form of myopathy with inflammation in those over the age of 50 in Western countries, is an intractable and progressive skeletal muscle disease of unknown cause and without effective treatment. Muscle biopsy typically reveals endomysial inflammation, invasion of mononuclear cells into non-necrotic
Masashi, Aoki, Naoki, Suzuki
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[Sporadic inclusion body myositis and amyloid].

Brain and nerve = Shinkei kenkyu no shinpo, 2014
Sporadic inclusion body myositis (sIBM) is an intractable and progressive skeletal muscle disease of unknown etiology and without effective treatment. While the etiology is still unknown, however, genetic factors, aging, life style, and environmental factors may be involved.
Masashi, Aoki, Naoki, Suzuki
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Myositis with prominent B cell aggregates may meet classification criteria for sporadic inclusion body myositis

Neuromuscular Disorders, 2023
François Grand'Maison +2 more
exaly

Sporadic Inclusion Body Myositis

2009
Alexander K. C. Leung +150 more
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Myositis, Sporadic Inclusion Body

2009
Mark Oette +194 more
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medicine
myositis
inflammation

idiopathic inflammatory myopathies
dermatomyositis
inclusion body myositis

polymyositis
immune-mediated necrotizing myopathy
inflammatory myopathies